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N,N-dimethyl-4-[6-(2-phenoxyphenyl)imidazo[1,2-a]pyrazin-3-yl]benzamide ID: ALA3730520
PubChem CID: 117769377
Max Phase: Preclinical
Molecular Formula: C27H22N4O2
Molecular Weight: 434.50
Molecule Type: Small molecule
This compound is available for customization.
Associated Items:
Names and Identifiers Canonical SMILES: CN(C)C(=O)c1ccc(-c2cnc3cnc(-c4ccccc4Oc4ccccc4)cn23)cc1
Standard InChI: InChI=1S/C27H22N4O2/c1-30(2)27(32)20-14-12-19(13-15-20)24-16-29-26-17-28-23(18-31(24)26)22-10-6-7-11-25(22)33-21-8-4-3-5-9-21/h3-18H,1-2H3
Standard InChI Key: NZLNJLZNMUKNJM-UHFFFAOYSA-N
Molfile:
RDKit 2D
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1.7138 -1.2033 0.0000 N 0 0 0 0 0 0 0 0 0 0 0 0
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-4.9143 0.7422 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
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3.6621 2.8384 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
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-2.3239 3.7512 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
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-3.6328 5.9946 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
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M END Associated Targets(Human) Associated Targets(non-human) Molecule Features Natural Product: NoOral: NoChemical Probe: NoParenteral: NoMolecule Type: Small moleculeTopical: NoFirst In Class: NoBlack Box: NoChirality: NoAvailability: NoProdrug: No
Drug Indications MESH ID MESH Heading EFO IDs EFO Terms Max Phase for Indication References
Mechanisms of Action Mechanism of Action Action Type target ID Target Name Target Type Target Organism Binding Site Name References
Calculated Properties Molecular Weight: 434.50Molecular Weight (Monoisotopic): 434.1743AlogP: 5.56#Rotatable Bonds: 5Polar Surface Area: 59.73Molecular Species: NEUTRALHBA: 5HBD: ┄#RO5 Violations: 1HBA (Lipinski): 6HBD (Lipinski): ┄#RO5 Violations (Lipinski): 1CX Acidic pKa: ┄CX Basic pKa: 3.01CX LogP: 3.94CX LogD: 3.94Aromatic Rings: 5Heavy Atoms: 33QED Weighted: 0.36Np Likeness Score: -1.16
References 1. (2014) Nitrogen bicyclic compounds as inhibitors for Scyl1 and Grk5, 2. Antonova-Koch Y, Meister S, Abraham M, Luth MR, Ottilie S, Lukens AK, Sakata-Kato T, Vanaerschot M, Owen E, Jado JC, Maher SP, Calla J, Plouffe D, Zhong Y, Chen K, Chaumeau V, Conway AJ, McNamara CW, Ibanez M, Gagaring K, Serrano FN, Eribez K, Taggard CM, Cheung AL, Lincoln C, Ambachew B, Rouillier M, Siegel D, Nosten F, Kyle DE, Gamo FJ, Zhou Y, Llinás M, Fidock DA, Wirth DF, Burrows J, Campo B, Winzeler EA.. (2018) Open-source discovery of chemical leads for next-generation chemoprotective antimalarials., 362 (6419): [PMID:30523084 ] [10.1126/science.aat9446 ]